Co-curing agents for epoxy resins

• US 4,268,656 A
• Filed: 01/16/1980
• Issued: 05/19/1981
• Est. Priority Date: 01/16/1980
• Status: Expired due to Term

• Current Assignee: National Starch And Chemical Corporation (Ingredion Incorporated)
• Original Assignee: National Starch And Chemical Corporation (Ingredion Incorporated)
• Inventors: Schoenberg, Jules E., Ray-Chaudhuri, Dilip K., Chiao, Wen B.
• Primary Examiner(s): Nielsen, Earl A.
• Application Number:
  US06/112,496
• Time in Patent Office: 489 Days
• Field of Search: 528/96, 528/103, 528/111, 528/365, 528/407, 528/361, 528/367
• US Class Current: 528/103
• CPC Class Codes: C08G 59/184 with amines
• CPC Class Codes: C08G 59/4021 Ureas; Thioureas; Guanidines; Dicyandiamides
• CPC Class Codes: C08G 59/4035 Hydrazines; Hydrazides
• CPC Class Codes: C08G 59/5073 having two nitrogen atoms in the ring

Abstract

A N-substituted piperazine or N-substituted homopiperazine adduct with a polyepoxide is used as a co-curing agent in epoxy resin systems containing a polyepoxide and a known curing agent such as dicyandiamide, a carboxylic acid anhydride, or a dihydrazide. The preferred adducts have a ratio of epoxy groups to secondary amino groups of between 1.2:1 and 3:1. The preferred polyepoxides are polyglycidyl ethers of 4,4'"'"'-isopropylidenediphenol (bisphenol A). Suitable adducts are prepared from N-methyl-, N-(2-hydroxyethyl)-, N-octyl-, N-phenyl- and N-benzyl piperazine and N-methyl homopiperazine.

Claims

1. A unitary, storable, heat-curable epoxy resin system, which comprises a polyepoxide and a curing amount of a combination comprising (1) an epoxy curing agent and (2) a co-curing agent prepared by reacting (a) a polyepoxide with (b) a N-substituted piperazine or a N-substituted homopiperazine, wherein said piperazine is substituted with an alkyl, substituted alkyl, cycloalkyl, aryl or aralkyl group of up to 12 carbon atoms and said homopiperazine is substituted with an alkyl group of up to 3 carbon atoms, said co-curing agent having a ratio of epoxy groups to secondary amino groups of at least 0.8:

1.

2. The system of claim 1, wherein said polyepoxides are aromatic polyepoxides and said co-curing agent has a mole ratio of epoxy groups to secondary amino groups of between 1.2:

1 and 3;

1.

3. The system of claim 2, wherein said polyepoxides are glycidyl polyethers of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent weight of from 175 to 4000.

4. The system of claim 1, wherein said epoxy curing agent is dicyandiamide.

5. The system of claim 1, wherein said epoxy curing agent is a carboxylic acid ahydride.

6. The system of claim 5, wherein said carboxylic acid anhydride is 1,2-cyclohexane dicarboxylic acid anhydride, succinic anhydride, phthalic anhydride, or bicyclo(2.2.1)-heptene-2,3-dicarboxylic anhydride.

7. The system of claim 1, wherein said epoxy curing agent is a dihydrazide.

8. The system of claim 7, wherein said dihydrazide is azelayl dihydrazide or isophthalyl dihydrazide.

9. The system of claim 1, wherein said co-curing agent is prepared from a glycidyl polyether of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 600 and and a compound selected from the group consisting of N-methyl piperazine, N-(2-hydroxyethyl) piperazine, N-octyl piperazine, N-phenyl piperazine, N-benzyl piperazine, and N-methyl homopiperazine, said co-curing agent being employed in amounts of from 0.05 to 20% by weight, based on said polyepoxide.

10. The system of claim 9, wherein said co-curing agent is employed in amounts of from 0.5 to 10% by weight, based on said polyepoxide.

11. A process for converting a polyepoxide into an insoluble, infusible product, which comprises heating said polyepoxide at an elevated temperature with a curing amount of a combination comprising (1) an epoxy curing agent and (2) a co-curing agent prepared by reacting (a) a polyepoxide with (b) a N-substituted piperazine or a N-substituted hompiperazine, wherein said piperazine is substituted with an alkyl, substituted alkyl, cycloalkyl, aryl or aralkyl group of up to 12 carbon atoms and said homopiperazine is substituted with an alkyl group of up to 3 carbon atoms and said co-curing agent has a ratio of epoxy groups to secondary amino groups of at least 0.8:

1, said heating taking place at a temperature above 50°

C. for a time sufficient to complete the cure.

12. The process of claim 11, wherein said polyepoxides are glycidyl polyethers of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 4000.

13. The process of claim 11, wherein said epoxy curing agent is dicyandiamide.

14. The process of claim 11, wherein said epoxy curing agent is a carboxylic acid anhydride selected from the group consisting of 1,2-cyclohexane dicarboxylic acid anhydride, succinic anhydride, phthalic anhydride, and bicyclo (2.2.1)-heptene-2,3-dicarboxylic anhydride.

15. The process of claim 11, wherein said epoxy curing agent is a dihydrazide selected from the group consisting of azelayl dihydrazide and isophthalyl dihydrazide.

16. The process of claim 11, wherein said co-curing agent is prepared from a glycidyl polyether of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 600 and a compound selected from the group consisting of N-methyl piperazine, N-(2-hydroxyethyl) piperazine, N-octyl piperazine, N-phenyl piperazine, N-benzyl piperazine, and N-methyl homopiperazine, said co-curing agent has a mole ratio of epoxy groups to secondary amino groups of between 1.2:

1 and 1;

3, and said co-curing agent is employed in amounts of from 0.05 to 20%, based on said polyepoxide.

17. The process of claim 16, wherein said co-curing agent is employed in amounts of from 0.5 to 10%, based on said polyepoxide.

18. A process for making a thermoset article of manufacture using a heat-curable epoxy resin adhesive comprising a polyepoxide, an epoxy curing agent, and a co-curing agent prepared by reacting (a) a polyepoxide with (b) a N-substituted piperazine or a N-substituted homopiperazine, wherein said piperazine is substituted with an alkyl, substituted alkyl, cycloalkyl, aryl or aralkyl group of up to 12 carbon atoms and said homopiperazine is substituted with an alkyl group of up to 3 carbon atoms, said co-curing agent having a ratio of epoxy groups to secondary amino groups of at least 0.8:

1.

19. The process of claim 18, wherein said polyepoxide is a glycidyl polyether of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 4000;

said epoxy curing agent is selected from the group consisting of dicyandiamide, 1,2-cyclohexane dicarboxylic acid anhydride, succinic anhydride, phthalic anhydride, and bicyclo (2.2.1)-heptene-2,3-dicarboxylic anhydride; and

said co-curing agent is prepared from a glycidyl polyether of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 600 and a compound selected from the group consisting of N-methyl piperazine, N-(2-hydroxyethyl)-piperazine, N-octyl piperazine, N-phenyl piperazine, N-benzyl piperazine, and N-methyl homopiperazine and said co-curing agent has a mole ratio of epoxy groups to secondary amino groups of between 1.2;

1 and 3;

1.

20. A composition of matter, useful as a co-curing agent for polyepoxides, which comprises the reaction product of a glycidyl polyether of 4,4'"'"'-isopropylidenediphenol having an epoxide equivalent of from 175 to 600 with a N-substituted piperazine or a N-substituted homopiperazine, wherein said piperazine is substituted with an alkyl, substituted alkyl, cycloalkyl, aryl, or aralkyl group of up to 12 carbon atoms and said homopiperazine is substituted with an alkyl group of up to 3 carbon atoms, wherein said reaction product has a mole ratio of epoxy groups to secondary amino groups of between 0.8:

1 and 4;

1.

21. The composition of matter of claim 20, wherein said piperazine is N-methyl piperazine, N-(2-hydroxyethyl) piperazine, N-octyl piperazine, N-phenyl piperazine or N-benzyl piperazine and said homopiperazine is N-methyl homopiperazine.

22. The process for preparing the composition of claim 20, which comprises mixing said glycidyl polyether with said N-substituted piperazine or said N-substituted homopiperazine.